Technomed Europe
Technomed Europe holds FDA 510(k) medical device clearances, first cleared 1999, most recent 2026, with 3 FDA device recalls on record.
Top product codes for Technomed Europe
FDA recalls by Technomed Europe
- Z-3131-2024 — NEUROSIGN Disposable Stimulating Dissector, REF 5888-00
- Z-1737-2022 — Disposable Subdermal Needle Electrode, Pt/lr, 12 x 0.40mm, product number TE/S46/638, 25 needles per package, sterile.
- Z-0465-2022 — Disposable Subdermal Needle Electrode, Corkscrew, Single Use, Sterile; Model Numbers TE/S50715-001-C, TE/S50725-001C, and TE/S50715-001.
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Technomed Europe
- K254183 — MR Conditional Cup Electrodes
- K253581 — Disposable Concentric Needle Electrode 0.30x25mm Red (TE/B50700-001) +5 more
- K241045 — Disposable Subdermal Needle Electrode, Corkscrew
- K130136 — DISPOSABLE AND REUSABLE CONCENTRIC NEEDLE ELECTRODES,DISPOSABLE AND REUSABLE SUBDERMAL NEEDLE ELECTRODES,
- K121257 — LARYNGEAL ELECTRODE
- K110422 — SURGICAL STIMULATORS
- K073532 — DISPOSABLE ADHESIVE SURFACE ELECTRODES, DISC ELECTRODES
- K072016 — CUP ELECTRODES, GOLD, REUSABLE, SILVER, REUSABLE; CUP ELECTRODES SILVER/SILVER CHLORIDE REUSABLE
- K063729 — DISPOSABLE PEDICLE SCREW PROBE, MODEL 3603-00
- K062437 — DISPOSABLE HYPODERMIC EMG NEEDLE ELECTRODE TECHNOMED EUROPE VERSION AND PRIVATE LABELED
- K050325 — DISPOSABLE CONCENTRIC PROBE, DISPOSABLE BIPOLAR PROBE, DISPOSABLE MONOPOLAR PROBE
- K042375 — SMK, CX, CXE, RCN
- K990015 — ELECTRODE NEEDLES
Data sourced from openFDA. This site is unofficial and independent of the FDA.